Table 1.
In silico ADME parameters for PADPZ.
| Water Solubility | |
| Log S (ESOL) | −4.50 |
| Solubility | 1.38 × 10−2 mg/mL; 3.20 × 10−2 mol/L |
| Class | Moderately soluble |
| Pharmacokinetics | |
| GI absorption | High |
| BBB permeant | Yes |
| P-gp substrate | Yes |
| CYP1A2 inhibitor | No |
| CYP2C19 inhibitor | No |
| CYP2C9 inhibitor | No |
| CYP2D6 inhibitor | Yes |
| CYP3A4 inhibitor | Yes |
| Lipinski | Yes; 0 violation |